Yevgenya Kraytsberg

2.5k total citations · 1 hit paper
27 papers, 1.9k citations indexed

About

Yevgenya Kraytsberg is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Yevgenya Kraytsberg has authored 27 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Yevgenya Kraytsberg's work include Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (9 papers) and Genetic Neurodegenerative Diseases (8 papers). Yevgenya Kraytsberg is often cited by papers focused on Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (9 papers) and Genetic Neurodegenerative Diseases (8 papers). Yevgenya Kraytsberg collaborates with scholars based in United States, United Kingdom and Russia. Yevgenya Kraytsberg's co-authors include Konstantin Khrapko, Elena Kudryavtseva, Neil W. Kowall, Changiz Geula, Ann C. McKee, Wolfram S. Kunz, Konstantin K. Ebralidse, Jan Vijg, David A. Clayton and John Vissing and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Yevgenya Kraytsberg

26 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons

2006 712 citations Yevgenya Kraytsberg, Elena Kudryavtseva et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Yevgenya Kraytsberg United States	18	1.5k	482	364	264	237	27	1.9k
Carl E.G. Bruder Sweden	19	2.2k 1.5×	534 1.1×	244 0.7×	252 1.0×	548 2.3×	33	3.2k
Péter L. Nagy United States	26	1.5k 1.0×	97 0.2×	241 0.7×	327 1.2×	242 1.0×	58	2.3k
Scott Noggle United States	27	2.7k 1.7×	74 0.2×	581 1.6×	106 0.4×	575 2.4×	53	3.4k
Dmitry Ivanov United States	27	1.6k 1.0×	107 0.2×	275 0.8×	118 0.4×	316 1.3×	62	2.4k
Penelope E. Bonnen United States	19	1.8k 1.2×	250 0.5×	1.2k 3.3×	463 1.8×	120 0.5×	37	2.4k
Chantal M. Longo-Guess United States	18	1.5k 1.0×	63 0.1×	234 0.6×	71 0.3×	173 0.7×	24	2.2k
Ki Wha Chung South Korea	29	1.2k 0.8×	113 0.2×	1.2k 3.3×	349 1.3×	112 0.5×	152	2.5k
Parsa Kazemi‐Esfarjani United States	16	2.4k 1.6×	66 0.1×	1.8k 4.8×	476 1.8×	124 0.5×	17	2.9k
Conceição Bettencourt United Kingdom	24	816 0.5×	64 0.1×	681 1.9×	404 1.5×	115 0.5×	73	1.4k
Christian P. Hamel France	26	2.0k 1.3×	144 0.3×	366 1.0×	66 0.3×	78 0.3×	71	2.4k

Countries citing papers authored by Yevgenya Kraytsberg

Since Specialization

Citations

This map shows the geographic impact of Yevgenya Kraytsberg's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yevgenya Kraytsberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yevgenya Kraytsberg more than expected).

Fields of papers citing papers by Yevgenya Kraytsberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yevgenya Kraytsberg. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yevgenya Kraytsberg. The network helps show where Yevgenya Kraytsberg may publish in the future.

Co-authorship network of co-authors of Yevgenya Kraytsberg

This figure shows the co-authorship network connecting the top 25 collaborators of Yevgenya Kraytsberg. A scholar is included among the top collaborators of Yevgenya Kraytsberg based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Yevgenya Kraytsberg. Yevgenya Kraytsberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Popadin, Konstantin, Konstantin Gunbin, Leonid Peshkin, et al.. (2022). Mitochondrial Pseudogenes Suggest Repeated Inter-Species Hybridization among Direct Human Ancestors. Genes. 13(5). 810–810. 9 indexed citations

Safdar, Adeel, Sofia Annis, Yevgenya Kraytsberg, et al.. (2016). Amelioration of premature aging in mtDNA mutator mouse by exercise: the interplay of oxidative stress, PGC-1α, p53, and DNA damage. A hypothesis. Current Opinion in Genetics & Development. 38. 127–132. 34 indexed citations

Kraytsberg, Yevgenya, Xinhong Guo, Daniel J. Ehrlich, et al.. (2015). Quantitation of Mitochondrial DNA Deletions Via Restriction Digestion/Long-Range Single-Molecule PCR. Methods in molecular biology. 1351. 33–46. 4 indexed citations

Amabile, Giovanni, Robert S. Welner, César Nombela‐Arrieta, et al.. (2012). In vivo generation of transplantable human hematopoietic cells from induced pluripotent stem cells. Blood. 121(8). 1255–1264. 160 indexed citations

Campbell, G., Yevgenya Kraytsberg, Kim J. Krishnan, et al.. (2012). Clonally expanded mitochondrial DNA deletions within the choroid plexus in multiple sclerosis. Acta Neuropathologica. 124(2). 209–220. 31 indexed citations

Guo, Xinhong, Elena Kudryavtseva, Natalya D. Bodyak, et al.. (2010). Mitochondrial DNA deletions in mice in men: Substantia nigra is much less affected in the mouse. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797(6-7). 1159–1162. 18 indexed citations

Nicholas, Adeline K., João Pedro de Magalhães, Yevgenya Kraytsberg, et al.. (2010). Age-related gene-specific changes of A-to-I mRNA editing in the human brain. Mechanisms of Ageing and Development. 131(6). 445–447. 41 indexed citations

Nicholas, Alexander, Yevgenya Kraytsberg, Xinhong Guo, & Konstantin Khrapko. (2009). On the timing and the extent of clonal expansion of mtDNA deletions: Evidence from single-molecule PCR. Experimental Neurology. 218(2). 316–319. 22 indexed citations

Kraytsberg, Yevgenya, et al.. (2009). Collection of Isolated Cells for Studying Mitochondrial DNA Mutations Within Individual Cells. Methods in molecular biology. 554. 315–327. 3 indexed citations

10.

Kraytsberg, Yevgenya, et al.. (2009). Quantitative Analysis of Somatic Mitochondrial DNA Mutations by Single-Cell Single-Molecule PCR. Methods in molecular biology. 554. 329–369. 17 indexed citations

11.

Kraytsberg, Yevgenya, David K. Simon, Douglass M. Turnbull, & Konstantin Khrapko. (2009). Do mtDNA deletions drive premature aging in mtDNA mutator mice?. Aging Cell. 8(4). 502–506. 34 indexed citations

12.

Kraytsberg, Yevgenya, Alexander Nicholas, Pilar Caro, & Konstantin Khrapko. (2008). Single molecule PCR in mtDNA mutational analysis: Genuine mutations vs. damage bypass-derived artifacts. Methods. 46(4). 269–273. 13 indexed citations

13.

Kraytsberg, Yevgenya, Elena Kudryavtseva, Ann C. McKee, et al.. (2006). Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons. Nature Genetics. 38(5). 518–520. 712 indexed citations breakdown →

14.

Khrapko, Konstantin, et al.. (2006). Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging?. Aging Cell. 5(3). 279–282. 65 indexed citations

15.

Kraytsberg, Yevgenya & Konstantin Khrapko. (2005). Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations. Expert Review of Molecular Diagnostics. 5(5). 809–815. 57 indexed citations

16.

Khrapko, Konstantin, Konstantin K. Ebralidse, & Yevgenya Kraytsberg. (2004). Where and When Do Somatic mtDNA Mutations Occur?. Annals of the New York Academy of Sciences. 1019(1). 240–244. 10 indexed citations

17.

Khrapko, Konstantin, et al.. (2003). Clonal expansions of mitochondrial genomes: implications for in vivo mutational spectra. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 522(1-2). 13–19. 27 indexed citations

18.

Morozova, Nadya, Erin P. Forry, Ann Marie Zavacki, et al.. (2003). Antioxidant function of a novel selenoprotein in Drosophila melanogaster. Genes to Cells. 8(12). 963–971. 39 indexed citations

19.

Kraytsberg, Yevgenya, et al.. (2003). Mutation and intracellular clonal expansion of mitochondrial genomes: two synergistic components of the aging process?. Mechanisms of Ageing and Development. 124(1). 49–53. 38 indexed citations

20.

Kraytsberg, Yevgenya, et al.. (2002). mtLOH (mitochondrial loss of heteroplasmy), aging, and ‘surrogate self’. Mechanisms of Ageing and Development. 123(8). 891–898. 7 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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